Sunscreen
Product Images NDC 62932-214

10 FDA label images from Private Label Select Ltd Co · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Sunscreen (NDC 62932-214). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Private Label Select Ltd Co, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Back Label (Back Label)

Back Label (Back Label)
Drug Facts text panel for SUNSCREEN by Private Label Select Ltd CO, featuring active ingredient Zinc Oxide 20% and SPF 30. The panel includes purpose, uses, warnings, directions, sun protection measures, reapplication instructions, inactive ingredients, and other product information. The label mentions organic certified ingredients and advises on precautions and usage for sun protection.*
FDA Label Image

Dosage And Administration (Dosage And Administration)

Dosage And Administration (Dosage And Administration)
A text panel containing directions and sun protection measures for sunscreen use. It instructs to apply generously 15 minutes before sun exposure, notes children under 6 months should consult a doctor, and details protective practices such as limiting sun time, wearing protective clothing, and regularly reapplying sunscreen after swimming, sweating, towel drying, or every 2 hours.*
FDA Label Image

Front Label (Front Label)

Front Label (Front Label)
Label of Olita Mineral Sunscreen with SPF 30, featuring a light tan tint. The sunscreen is identified as broad spectrum and water resistant for 80 minutes. The label includes a reef safe indication, a wave graphic, and states it contains organic ingredients. Net weight is .5 oz (14 g). The product is labeled by Private Label Select Ltd CO.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Inactive Ingredients (Inactive Ingredients)
This text panel lists the inactive ingredients of a product labeled as SUNSCREEN by Private Label Select Ltd CO. It details various waxes, oils, butters, powders, and colorants including caprylic/capric triglyceride, sunflower seed oil, beeswax, carnauba wax, shea butter, castor seed oil, cocoa seed butter, aloe vera powder, mica, and iron oxides. Several ingredients are noted as certified organic.*
FDA Label Image

Indications And Usage (Indications And Usage)

Indications And Usage (Indications And Usage)
This text panel provides information on the uses of the product, stating it helps prevent sunburn and, when used as directed with other sun protection measures, decreases the risk of skin cancer and early skin aging caused by the sun. It also references directions for use.*
FDA Label Image

Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)

Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)
Text panel titled 'Drug Facts (continued)' advising to stop use and ask a doctor if a rash occurs, keep out of reach of children, and to get medical help or contact a Poison Control Center if the product is swallowed.*
FDA Label Image

Otc Active Ingredients (Otc Active Ingredients)

Otc Active Ingredients (Otc Active Ingredients)
Text panel showing active ingredients, specifically listing Zinc Oxide 20%. This panel is part of a product labeled as SUNSCREEN by Private Label Select Ltd CO.*
FDA Label Image

Otc Purpose Section (Otc Purpose)

Otc Purpose Section (Otc Purpose)
A drug facts panel section for a sunscreen product. The visible portion includes headings such as Purpose, Uses, and Warnings, along with text describing the product's purpose to act as sunscreen and details on use instructions and warnings. The label appears to provide standard consumer safety information.*
FDA Label Image

Warnings Part One (Warnings Part One)

Warnings Part One (Warnings Part One)
A warning panel advising not to use the product on damaged or broken skin and to keep it out of eyes when using the product. It also instructs to rinse with water to remove product if it gets in the eyes.*
FDA Label Image

Warnings Section Part Two (Warnings Part Two)

Warnings Section Part Two (Warnings Part Two)
Drug Facts panel excerpt advising to stop use and consult a doctor if rash occurs. It cautions to keep the product out of reach of children and to seek medical help or contact Poison Control Center if swallowed.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.